SCD Partner Letter to Leadership on SCD Stimulus Amendment
Tuesday, April 28, 2020
Dear Speaker Pelosi, Leader McConnell, Leader McCarthy, and Leader Schumer,
The undersigned organizations, all committed to improving outcomes for individuals with sickle cell disease (SCD), are gravely concerned about the impact COVID-19 is having on African Americans and Hispanics in the US and particularly, on individuals with SCD, who often live with long term heart and lung problems (multiple severe co-morbidities) and are at higher risk of life threatening complications if infected. As you consider legislative proposals for the next stimulus bill we ask that you include an authorization for the Centers for Medicare and Medicaid Services (CMS) to quickly develop a program for Medicare/Medicaid dual eligible and Medicaid beneficiaries to improve access to comprehensive outpatient care for individuals with SCD.
SCD is an inherited blood disorder that affects an estimated 100,000 Americans, primarily African Americans and Hispanics. Individuals with the disease produce abnormal hemoglobin which results in their red blood cells becoming rigid and sickle-shaped and causing them to get stuck in blood vessels and block blood and oxygen flow to the body. SCD complications include severe pain, stroke, acute chest syndrome (a condition that lowers the level of oxygen in the blood), organ damage, and in some cases premature death. The suppressed immune system and co-existing medical conditions occurring in individuals with SCD result in a much higher risk of severe complications stemming from infection with COVID-19.
Sadly, not enough individuals living with SCD are able to access the care of specialists or primary care physicians that understand the disease and have the resources to effectively treat those affected. Preventive care includes transfusions, lab tests, radiographic studies, and vaccines, which are critically needed to prevent infection or strokes, and to manage severe pain, in addition to needed treatment for COVID-related illness. Many necessary services cannot be provided by telehealth, so it has become increasingly difficult to manage the individuals with the disease in their homes and these people are fearful of going to emergency departments or a hospital for care. We worry that there are many individuals with SCD at home living in severe pain and worsening heart, lung, and renal disease.
An organized approach to primary and preventive care for individuals with SCD is desperately needed to improve the health and quality of life for this population. The model CMS program will focus on providing specialized and primary care in appropriate outpatient settings. With the recent
The undersigned organizations, all committed to improving outcomes for individuals with sickle cell
publication of clinical practice guidelines in sickle cell disease and approvals of new treatments for SCD and more in the pipeline, there is no better time than now to improve the SCD community’s access to state-of-the-art care.
We ask for your leadership on this issue by including in the next stimulus bill an authorization for CMS to develop a demonstration program to improve outpatient services under Medicare and Medicaid to this vulnerable population. During this time of crisis, it is critical to initiate this program.
Please consider all the organizations listed below as a resource and keep us apprised on how we can assist you. Thank you for your consideration. Thank you for your efforts to improve the lives of individuals with this debilitating disease.
American Society of Hematology
Sickle Cell Disease Association of America
American College of Emergency Physicians
American Medical Association
American Public Health Association
American Red Cross
American Society of Pediatric Hematology/Oncology
American Society for Apheresis
ASH Research Collaborative
Association of Public Health Laboratories
Bridges Pointe Sickle Cell Foundation
Cayenne Wellness Center
Colorado Sickle Cell Association
Dreamsickle Kids Foundation
Emergency Department Sickle Cell Care Coalition (EDSC3)
Foundation for Sickle Cell Disease Research
Global Blood Therapeutics Inc. (GBT)
Heart of Gold Sickle Cell Foundation of Northern Virginia
Howard University Center for Sickle Cell Disease
International Association of Sickle Cell Nurses and Professional Associates (IASCNAPA) LIVING with Sickle Cell, Inc.
National Black Leadership Commission on Health
National Institute for Children's Health Quality (NICHQ)
National Medical Association
New York State Advocacy Network, Inc.
New York State Sickle Cell Advocacy Network, INC.
Newark Beth Israel Medical Center
North Alabama Sickle Cell Foundation, Inc.
Novartis Pharmaceuticals Corporation
Ohio Sickle Cell Affected Families Association SCDAA Miami-Dade County Chapter, Inc.
SCDAA Ohio Sickle Cell and Health Association Sick Cells
Sickle Cell 101
Sickle Cell Adult Provider Network
Sickle Cell Anemia Foundation of Oregon, Inc.
Sickle Cell Association – West Alabama Chapter, Inc.
Sickle Cell Association of Virginia, Inc.
Sickle Cell Awareness
Sickle Cell Disease Association of America Michigan Chapter
Sickle Cell Disease Association of America, Philadelphia/Delaware Valley Chapter Sickle Cell Disease Association of America, St. Petersburg Chapter, Inc.
Sickle Cell Disease Association of Broward County
Sickle Cell Disease Association of Illinois
Sickle Cell Disease Community Forum
Sickle Cell Foundation of Georgia, Inc.
Sickle Transplant Advocacy and Research Alliance (STAR)
Smile Sickle Cell Foundation
South Central PA Sickle Cell Council
Southeast Alabama Sickle Cell Association, Inc.
SSM Health Cardinal Glennon Children's Hospital
Thalassaemia International Federation
The Children's Sickle Cell Foundation, Inc.
The North Carolina Sickle Cell Disease Provider Consortium NCSCD-PC
The Sickle Cell Association of New Jersey
The Sickle Cell Disease Enterprise, Levine Cancer Institute, Atrium Health
The Sickle Cell Foundation of Tennessee
Thomas Jefferson University